ORPHA:576360
Acquired human prion disease
Synonyms: Infectious human prion disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired human prion disease | Infectious human prion disease |
| fr | Maladie à prion humaine acquise | Maladie à prion humaine infectieuse |
| de | Prionkrankheit, humane, erworbene Form | |
| es | Enfermedad por priones humanos adquirida | |
| it | Malattia umana acquisita da prioni | Malattia umana infettiva da prioni |
| nl | Verworven humane prionziekte | |
| pt | Doença de priões humana adquirida | |
| pl | Nabyta ludzka choroba prionowa | = en |
| cs | Získané lidské prionové onemocnění | = en |
| uk | Набута пріонна хвороба людини | Інфекційна пріонна хвороба людини |
| zh | 获得性人朊病毒病 | 感染性人朊病毒病 |
| tr | Edinsel insan prion hastalığı | Bulaşıcı insan prion hastalığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0035562 | E | validated | |
| UMLS | C5680357 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:56970Human prion disease
rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/576360
- This record as JSON: /data/d/576360.json